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Script assisted update of identifiers from ChemSpider, CommonChemistry and FDA for the Chem/Drugbox validation project - Updated: ChemSpiderID InChI InChIKey SMILES1. |
Script assisted update of identifiers from ChemSpider, CommonChemistry and FDA for the Chem/Drugbox validation project - Updated: StdInChI StdInChIKey. |
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| InChIKey = PIVQQUNOTICCSA-UHFFFAOYAV |
| InChIKey = PIVQQUNOTICCSA-UHFFFAOYAV |
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| SMILES1 = S=C(N)Nc2cccc1ccccc12 |
| SMILES1 = S=C(N)Nc2cccc1ccccc12 |
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| StdInChI = 1S/C11H10N2S/c12-11(14)13-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,(H3,12,13,14) |
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| StdInChIKey = PIVQQUNOTICCSA-UHFFFAOYSA-N |
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| CASNo=86-88-4 |
| CASNo=86-88-4 |
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| PubChem=736366 |
| PubChem=736366 |
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Revision as of 11:01, 29 November 2010
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| Names | |
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| IUPAC name
naphthalen-1-ylthiourea
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| Identifiers | |
3D model (JSmol)
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| Abbreviations | ANTU |
| ChemSpider | |
| ECHA InfoCard | 100.001.552 |
PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C11H10N2S | |
| Molar mass | 202.28 g/mol |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards
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Toxic |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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α-Naphthylthiourea (ANTU, Dirax) is an organosulfur compound. It is a derivative of thiourea and used as a rodenticide. It acts by inducing pulmonary edema and has relatively selective toxicity for rats.[1]
Safety
Currently, the substance is banned for use in plant protection by the UK government.[2]
References
- ^ Sipahi EY, Ozel Tekin I, Comert M, Barut F, Ustun H, Sipahi TH. Oxidized low-density lipoproteins accumulate in rat lung after experimental lung edema induced by alpha- naphthylthiourea (ANTU). Pharmacological Research. 2004 Dec;50(6):585-91. PMID 15501696
- ^ http://www.pesticides.gov.uk/approvals.asp?id=55